Alternatives to Net Station

Castor offers an intuitive and comprehensive platform for managing clinical trial data, focusing on electronic data capture (EDC), eConsent, and patient-reported outcomes (ePRO). The platform is optimized for decentralized trials, providing seamless tools for remote patient engagement and data collection. With real-time reporting, Castor helps researchers track trial progress and make data-driven decisions. The solution ensures compliance with industry regulations such as HIPAA, GDPR, and 21 CFR Part 11, making it ideal for life sciences organizations looking to enhance trial efficiency while maintaining high data integrity.

Medrio's Electronic Data Capture (EDC) platform and complimenting eClinical solutions such as ePRO, RTSM, eConsent, and Direct Data Capture (DDC) have been trusted by major pharmaceutical, biotech, CRO, animal health, medical device, and diagnostic companies since 2005. We are known for our easy-to-use solutions, delivering speed and simplicity to clinical trials of all phases, sizes, and complexities. Medrio users can build their databases in an average of 2.8 weeks with no programming required, make mid-study changes with just a few clicks of a mouse, and much more. From bolt-on capabilities to full-service offerings, Medrio offers flexible, modular solutions that give our customers exactly what they need – and none of what they don’t. Our innovative software, as well as the robust and flexible training and support resources we provide our customers, have earned us a 98% customer satisfaction rating.

ActiView is a comprehensive acquisition tool that showcases all ActiveTwo channels on a screen while saving the data in .BDF format to a network disk. The user-friendly layout allows for a swift assessment of data quality. This software is capable of acquiring EEG, ECG, and EMG signals, in addition to data from various external sensors like the AnalogInputBox (AIB), digital triggers sourced from the USB2 receiver, and other devices linked to the AD-box, including respiration monitors, GSR sensors, temperature gauges, ergometers, and plethysmographs. Users can select from multiple reference options, apply filters, and utilize downsampling features. Thanks to our unique single-buffered approach, the acquisition process remains stable and dependable even during multitasking, as the DMA transfer to a large intermediate ring buffer guarantees that no data is lost. ActiView is an open-source program developed in LabVIEW, making it an exceptionally flexible resource for researchers who wish to modify and enhance the software to suit their specific needs. Its adaptability and robust features position it as an invaluable asset in experimental setups.

OpenClinica is a leading provider of clinical data management software solutions. OpenClinica provides powerful tools to ensure that clinical trials are compliant and efficient. OpenClinica Enterprise, OpenClinica Participate and OpenClinica Randomize are the core products. OpenClinica is a powerful clinical trial platform that offers a wide range of tools for data collection, patient engagement, and study management. From electronic data capture (EDC) and eConsent to patient recruitment and real-time reporting, OpenClinica’s solutions automate and simplify the clinical trial process. With features like EHR-to-EDC integration and advanced reporting dashboards, the platform improves data accuracy, reduces delays, and enhances compliance. OpenClinica has been used in over 15,000 clinical studies, providing support for organizations around the globe, including government agencies and pharmaceutical companies, to conduct trials with confidence.

KoboToolbox offers a range of tools designed for the collection of field data in demanding situations. Our platform is completely free and open-source. The majority of our users include individuals engaged in humanitarian efforts, as well as aid workers and researchers operating in underdeveloped regions. Our development and research teams are located in Cambridge, MA, along with various other locations worldwide. Rapidly gathering dependable information during a humanitarian crisis, particularly after a significant natural disaster like a major earthquake or typhoon, is essential for protecting the lives of those most at risk. Unfortunately, the urgent needs of the affected population are often overlooked due to the lack of efficient methods for collecting and analyzing vital data. To fill this critical gap, KoboToolbox was established as a free and open-source resource for data collection and analysis during humanitarian emergencies and other difficult contexts. Our initiative relies entirely on the generous support of grants and collaborations with our partners, ensuring that we can continue to provide these vital tools to those who need them most. By facilitating quick access to actionable insights, we aim to empower communities to respond effectively to crises.

The BSCAN Standard serves as an independent capture solution or as part of a multi-tiered capture system. It comes in four different capacities: Personal, Low, Medium, and High Volume. One of the standout features of BSCAN is its robust customization options, enabling users to create intricate WorkFlows that include tailored screens, commands, key entry interfaces, and mouse-driven image processing capabilities. Its intuitive controls provide a variety of pre-defined screen layouts that ensure optimal image clarity for quality control, or users can opt to design their own custom layouts that focus solely on the functions they require for maximum efficiency. Setting up either a straightforward single scan and release station or an elaborate WorkFlow system with numerous stations is made easy with BSCAN's Wizard. Users can choose from a collection of sample capture WorkFlow templates or create their own, and the Wizard guides them through each step of the configuration process seamlessly. This level of flexibility and user support makes BSCAN an invaluable tool for any scanning operation, regardless of complexity.

Unlock unique insights with unparalleled freedom and adaptability using LabChart physiological data analysis software, which seamlessly integrates all your recording devices, enabling the simultaneous acquisition of biological signals from diverse sources while applying sophisticated calculations and visualizations in real time during your experiments. Quickly determine metrics such as Mean Arterial Pressure, Systolic Pressure, and Max dP/dt from your blood pressure recordings in mere moments. The Blood Pressure module offers remarkable ease of use and delivers rapid results, while our intuitive two-point calibration tool simplifies the conversion of voltage units to recognized measurement units efficiently. LabChart is designed to handle essential tasks effortlessly, with advanced functionalities remaining unobtrusive until they are needed. Tailor LabChart to your preferences by utilizing scripting and automation features available on Windows, and leverage custom arithmetic along with import and export capabilities across various formats for compatibility with other software applications. Experience a new level of efficiency and precision in your physiological data analysis with LabChart.

AI-driven analysis of medical imagery is complemented by sophisticated automation of clinical data processes. Offered as a web-based SaaS or an on-premise solution, UNITY has garnered global trust from leading medical technology firms and healthcare institutions for its ability to gather comprehensive, consistent, and compliant data. Its integrated modules for Patient-Reported Outcome Measures (PROM), electronic Case Report Forms (eCRF), and medical image analysis optimize essential data collection tasks, thereby facilitating quicker and more cost-effective clinical trials. RAYLYTIC's Imaging Core Lab brings decades of expertise in the precise, automated, and independent assessment of musculoskeletal structures and device efficacy in areas such as the spine, hip, and knee, providing clients with unmatched analytical and operational assistance. This advanced capability ensures that medical professionals can rely on high-quality data to inform their decision-making processes, ultimately improving patient outcomes.

ODK enables the creation of robust offline forms for data collection in any location you require. Join the ranks of prominent social impact organizations utilizing ODK to drive positive change in the world. Each month, millions rely on ODK for their data collection needs due to its versatility and accessibility. This platform boasts a variety of features that enhance your data gathering experience, including the ability to incorporate photos, GPS tracking, conditional logic, calculations, external data sources, support for multiple languages, and much more. Users can choose between the mobile app and the web interface, with automatic syncing of forms and submissions occurring whenever an internet connection is available. You can easily export your data or integrate it with applications like Excel, Power BI, or R for real-time dashboards. ODK has established itself as a benchmark in fields such as public health, global development, emergency response, and environmental monitoring. Countless organizations around the globe utilize ODK, collectively generating millions of submissions each month. As an open-source platform, ODK offers the flexibility to use it as is, personalize it to your needs, or explore other compatible options. While ODK can serve various purposes, our primary mission is to support social impact and empower individuals and organizations committed to enacting meaningful change in their communities. With its user-friendly interface and powerful capabilities, ODK stands out as a vital tool for anyone dedicated to making a difference through effective data collection.

When compared to other Electronic Data Capture (EDC) solutions available from companies like MediData, DataTrack, and Omnicomm, TrialStat stands out as the most comprehensive suite of study management tools that can effortlessly integrate with various external data sources, including electronic medical records (EMR), wearable devices, and both clinical and non-clinical information systems. TrialStat presents a cohesive platform that caters to all phases and categories of clinical trials. Our EDC suite is designed with a single sign-on feature and supports multiple tenants, incorporating modules for Randomization, Adjudication, Coding, Safety, Patient Diaries/ePRO, a Vendor Neutral Imaging Archive, an extensive Reporting and Analytics Portal, and tailored Machine Learning applications. With an emphasis on data analysis, TrialStat provides real-time reporting capabilities, on-demand data extracts, and analytics that span a single study, a program, or the entirety of your research portfolio, ensuring that all stakeholders receive pertinent, customized, and timely insights into every facet of study data while pinpointing areas of risk or potential delays. Additionally, the platform’s integration capabilities allow for improved collaboration among research teams, fostering a more efficient and effective trial management experience.

Our forms can be tailored to meet your unique requirements, workflows, and expected results. They are designed to be user-friendly and accessible for teams of any size. By converting your traditional paper forms into visually appealing digital documents in just a few minutes, you can enhance your productivity and cut expenses. There’s no need for lengthy training sessions! Culverdocs provides straightforward and efficient data entry solutions, guiding users throughout the entire process. With instant delivery, you won't have to wait for paper forms anymore, allowing you to concentrate on what truly matters. You can create and distribute high-quality reports that are beautifully customized to reflect your brand, as well as leverage custom dashboards for real-time data reporting and analysis. Our workflows ensure that information is sent to the appropriate departments without any hassle. Additionally, integrating Culverdocs into your current systems is a breeze. Our integration options allow you to link up with a variety of services or even create a tailored integration using any REST service, making adaptability a key feature of our platform. This flexibility empowers your organization to respond swiftly to evolving needs and utilize data more effectively.

Medidata's Rave EDC (Electronic Data Capture) stands out as the premier system for managing clinical trial data from sites, patients, and laboratories with unparalleled sophistication and security. Serving as the foundation of the Medidata Clinical Cloud™, it offers a comprehensive platform that integrates various processes, thereby eliminating the need for data reconciliation and providing insightful data analysis across different studies and functions. Users can efficiently oversee their roles, studies, and sites from a centralized dashboard that spans all Rave EDC and other Medidata Clinical Cloud products. This system helps in avoiding the pitfalls of duplicate study master data and inconsistencies, such as varying IDs for the same sites across different applications. At the core of Medidata’s cohesive approach to Clinical Data Capture and Management, Rave EDC facilitates the seamless aggregation and reconciliation of data from diverse sources, including Medidata eConsent, Medidata eCOA, MyMedidata, Rave RTSM, Rave Imaging, and Sensor Cloud; it also enhances data review and analysis through advanced tools like Rave TSDV and Medidata Detect. With these capabilities, Rave EDC not only simplifies data management but also empowers clinical researchers to make informed decisions based on reliable and comprehensive data insights.

BLU DELTA is an innovative invoice capturing application that employs genuine AI technology for seamless handling of digital receipts and automation processes. It is designed for professionals, offering instant and user-friendly functionality. Thanks to real AI, lead times are minimized and acquisition expenses are decreased, with no need for setup or training, resulting in immediate improvements in recognition rates. Whether through a cloud-based solution or an on-site option, and accessible via API or web interface, it transforms your digitization efforts into a valuable asset rather than just relying on basic OCR technology. Its standout feature includes an impressive recognition accuracy of up to 99% for various invoice formats, even those that are unfamiliar, easing the workload on your employees through enhanced automation. Additionally, the service offers forecasts upon request. A practical licensing structure and straightforward setup contribute to lower costs, ensuring that your company sees a swift return on investment. Clients also benefit from ongoing optimization and support, which are included at no extra charge. The BLU DELTA Capture Service can be deployed either as an MS Azure cloud solution or a local installation, with the assurance that your company’s data remains secure in either scenario. This advanced solution not only streamlines operations but also positions your business advantageously for future growth.

Encapsia continues to push the boundaries of modern concepts, and is already revitalizing clinical trials with the most flexible and efficient system. Responsive image Encapsia was built in the age of smart phones and leverages modern concepts to revitalize clinical trials. Encapsia eSource is available for direct data capture (DDC). It's the same system that provides medical coding, third-party data Loads, and industry-leading data visualisations. Encapsia is the most powerful and innovative system that allows you to collect and manage clinical trial data. Live is real. All data are available immediately after being entered. This gives you the ability to monitor trial progress and make informed management decisions.

DFnet is a company specializing in healthcare technology that delivers eClinical solutions such as electronic data capture, eSource, and comprehensive data management services. We enhance clinical trials globally by providing increased flexibility, improved data quality, and enhanced efficiency. Our platform allows for data collection from various sources, including paper CRFs, EDC, and other electronic systems, along with online and offline tablet entries and ePRO. You can either set up our system on your premises or utilize our secure cloud hosting options. Our advanced optical recognition technology accelerates SDV and RBM processes, significantly reducing the time required for manual data entry. Designed for optimal adaptability in multi-center studies, our web-based data capture system makes data from any source readily accessible in a centralized real-time platform. This capability ensures that researchers can make informed decisions quickly and efficiently, ultimately improving the overall conduct of clinical trials.

Any organization that accepts checks as a payment method can take advantage of AQ2 Remittance. This solution is adaptable for companies that handle a modest volume of 25 to 50 checks each day, scaling up to accommodate hundreds or even thousands of checks on a daily basis. By utilizing advanced check capture technology, businesses can drastically lower their operational and staffing expenses. AQ2 Remittance enables users to swiftly send check images and pertinent information electronically, eliminating the need for couriers or frequent trips to a local bank branch. In addition, the burdensome expenses associated with manually recording check amounts on deposit slips, conducting manual research, and distributing physical copies are effectively eliminated. This comprehensive check capture and electronic deposit service is designed specifically for businesses. With AQ2 Remittance, you can seamlessly capture data for efficient uploading into your accounts receivable system, enhancing overall productivity and accuracy. Ultimately, this innovative solution streamlines financial operations, freeing up valuable resources for other critical business activities.

AnjuEPS stands out as a premier solution for eSource and site automation, specifically crafted to enhance the efficiency of early-phase clinical trials, encompassing everything from the recruitment of volunteers to the final submission of studies. By capturing data directly from medical devices and implementing real-time edit checks, it guarantees the accuracy of data while eliminating reliance on traditional paper sources. The platform enhances safety monitoring with real-time alerts for out-of-range values and provides insights through historical safety data, ultimately facilitating improved management of volunteer safety. Its user-friendly Design & Build Module significantly accelerates the study setup process, which in turn helps lower both time and financial expenditures. Among its notable features are ad hoc reporting capabilities, sample tracking for intricate pharmacokinetic and pharmacodynamic activities, and comprehensive modules for recruitment and pharmacy management. With AnjuEPS, the collection of clinical data is not only efficient but also characterized by high levels of accuracy and transparency, making it an invaluable resource for clinical researchers. The solution's ongoing updates ensure that it remains at the forefront of technological advancements in the clinical trial landscape.

The genuine open-source electronic data capture (EDC) system for clinical research originated from a collaborative effort by volunteers with diverse expertise, including academia, clinical research services, and the IT sector. Today, this initiative is actively utilized by various academic institutions, hospitals, and emerging companies or startups, showcasing its widespread acceptance and adaptability in the field. This collaborative approach has fostered innovation and efficiency in the data collection process for clinical studies.

Gain deep insights into on-the-ground situations through top-tier mobile data collection tools available anytime, anywhere. The Dharma Platform offers a highly adaptable, user-focused system that transforms continuous data collection into actionable insights for every team member, regardless of their level of analytical expertise. This comprehensive data solution streamlines workflows, allowing you to focus on what truly matters: making a positive impact in the world. You can effortlessly create advanced, no-code applications for data collection that can be utilized globally, irrespective of location. From basic surveys to intricate data sets, Dharma Platform simplifies the process of designing, deploying, managing, and analyzing extensive survey data in real-time. Securely enroll, capture, and update individual records even in resource-limited settings. Thanks to our mobile capabilities and innovative online/offline functions, Dharma Platform optimizes your team's time and resources, enabling them to prioritize case management over paperwork. Ultimately, this powerful tool empowers organizations to enhance their operational efficiency and drive meaningful change.

Zelta is a cloud-powered platform for unified clinical data management and acquisition, designed to streamline and enhance clinical trial processes. Its modular architecture adapts to the unique demands of each study, enabling faster and more efficient outcomes. With capabilities such as electronic data capture, clinical operations management—including randomization and trial supply tracking—clinical trial management, and electronic trial master file functionality, Zelta supports comprehensive study oversight. It also enhances patient and provider engagement with electronic clinical outcome assessments and e-consent solutions. Built for studies across all phases, therapeutic areas, and global regions, Zelta offers an intuitive user experience with secure single sign-on access from anywhere. Its flexible and scalable design allows for seamless customization and integration with both native and third-party technologies, ensuring adaptability to diverse research needs.

Explore the realm of Technology Sustainability through comprehensive Content Services. Digitally capture and oversee documents, cases, records, and digital resources effectively. Enhance Process Management by automating workflows and processes with innovative AI-driven solutions. Ensure robust Data Governance by keeping up with cutting-edge technologies in cognitive search and analytics. In the Public Sector, leverage the newest technologies to foster advancements in institutions, promoting a positive influence on citizens, businesses, and communities as a whole. In Healthcare, enable medical personnel to deliver patient-focused services using a range of digital solutions, while also optimizing daily administrative and operational tasks. For the Oil & Gas sector, oversee vital information and sustain assets through the adoption of digital transformation, implementing successful strategies for profitable operations. In the realm of Engineering & Construction, utilize a range of automation tools from Intalio to efficiently manage engineering documentation and enhance processes within construction projects, ensuring a streamlined workflow throughout. This integration of technology across various sectors not only enhances operational efficiency but also drives innovation.

B2W Inform creates reports, dashboards, and alerts using electronic forms and additional sources, providing precise data that enhances operational efficiency, safety, quality, and financial results. The platform allows for quick and effortless creation and management of tailored forms, empowering contractors to eliminate outdated paper processes while collecting more comprehensive data in real time, accessible from any location and on any device. This transition to digital solutions not only streamlines workflows but also ensures that critical information is always at hand for informed decision-making.

When creating an application designed to capture screen activities and save them as WMV or AVI movie files, consider utilizing the Bytescout Screen Capturing SDK to seamlessly integrate screen video capturing capabilities. This SDK enables you to produce high-quality recordings of your desktop, complete with audio, mouse movements, and clicks. By using just a few lines of code with the ActiveX/COM object, you can effectively enhance your application with screen video capture features. It offers three distinct interfaces for screen video capturing: an ActiveX-based screen recorder, a DirectShow Filter, and a Virtual Camera, catering to both basic and advanced needs. Additionally, it includes a DirectShow Source Filter for developers working on sophisticated video applications. The SDK supports various video formats, including WMV, AVI, and lossless AVI via the included Bytescout Lossless Video Codec. During the recording process, it highlights the cursor with a hot-spot effect and visually animates mouse clicks, ensuring that both the cursor and clicks are easily identifiable in the final video output. This makes it an ideal choice for creating instructional videos and tutorials that require clear visual representation of user actions.

Sofpromed specializes in providing electronic data capture (EDC) solutions tailored for companies in the biotechnology, pharmaceutical, and medical device sectors involved in clinical trials ranging from phases I to IV. An EDC system serves as a software platform that facilitates the collection, validation, and exportation of data gathered during clinical studies. The EDC software developed by Sofpromed is utilized in clinical trials globally, spanning a diverse range of therapeutic fields such as oncology, hematology, cardiovascular health, metabolic disorders, central nervous system (CNS) issues, dermatology, infectious diseases, respiratory conditions, and pain management, among others. It boasts a user-friendly design that is simple and intuitive, allowing for rapid data entry and easy navigation. The platform also incorporates robust features such as access control and data encryption to ensure data security. Being fully web-based, it eliminates the need for any installations, providing convenience and efficiency. Additionally, it offers daily data backups and uninterrupted service, making it reliable for users. The system is compatible across various devices, browsers, and operating systems, enhancing its accessibility. It includes integrated monitoring, data management, and reporting functionalities, ensuring compliance with HIPAA, GCP, and 21 CFR standards. Furthermore, Sofpromed offers a convenient billing structure with a monthly flat rate, making it a practical choice for clinical trial needs. Overall, its comprehensive features and user-centric design make it an essential tool for conducting efficient and compliant clinical trials.

Clinical research is a time-consuming and demanding task. This puts a lot of pressure on the project team and makes it difficult to manage everything. The solution was designed to save you time when it comes to electronic data capture in clinical trials. Our data management department provides everything you need to collect clinical data. This will allow you to spend your time on what is most important. We can implement non-usual features or unique project-specific requirements. The EDC system is also flexible in budget terms. It is well-suited for low-budget clinical research. Our team has fully configured the Electronic Data Capture tool to meet your project requirements. Don't waste your time on system validation and configuration. The EDC system source code as well as the database are stored in the European Datacenter, or in any other country you choose. Multilevel backup also ensures the safety of clinical data.

Extracting business information from various sources such as printed or handwritten documents, forms, checks, invoices, emails, and more is a crucial task. This process can automatically convert unstructured customer data into a structured and digital format that is ready for business use. Once processed, the valuable data can be exported seamlessly into enterprise systems, databases, lines of business, or integrated into existing workflows. Despite the ongoing digitization and automation trends, paper remains a prevalent component in business operations worldwide. Many large corporations and organizations continue to face challenges with disorganized physical and digital documents that hinder their workflow efficiency. Significant time and resources are often dedicated to implementing automated solutions that still necessitate human intervention for data processing, which can ultimately diminish productivity and inflate costs. Consequently, businesses frequently find themselves in a position where they must sacrifice either cost-effectiveness, speed, accuracy, or the confidentiality of their data. The need for an effective solution that addresses these issues is more pressing than ever.

BIS, a company that has 35 years of experience in developing and delivering innovative technology, built Grooper from the ground up. Grooper is an intelligent data processing and digital data integration tool that allows organizations to extract meaningful information out of paper/electronic documents, and other unstructured data. The platform combines advanced image processing, capture technology and machine learning with optical character recognition to enrich data and embed human comprehension. Grooper is a foundation for many industry-first solutions, including in healthcare, financial services and education.

Flask Data equips life science research and development teams with timely clinical data and solutions for patient safety. The Flaskdata.io cloud API platform streamlines data collection applications for patients, researchers, site coordinators, connected devices, and pharmaceuticals. Our offerings in data management and safety oversight are designed to mitigate risks related to clinical data integrity, patient well-being, and adherence to protocols. The Flaskdata.io platform is not only automated but also scalable and responsive to the specific requirements of your clinical trials. Flask Data is a tech firm that focuses on clinical data oversight and management. We excel in delivering optimal solutions that ensure the highest quality of clinical data while prioritizing patient safety. Recognizing that there is no universal solution applicable to all clinical trials, we dedicate ourselves to thoroughly understanding your distinctive challenges. Collaborating closely with your team, we strive to create tailored solutions that meet your needs for high-quality clinical data and enhanced patient safety, ultimately driving the success of your research initiatives.

Cloudbyz EDC, a cloud-native application with an intuitive user interface, is designed to store and effectively manage clinical data throughout the life cycle of a clinical trial. Our innovative solution allows clinical research teams the ability to collect, analyze and manage clinical data that is of varying complexity and size. Create your study without coding, using an interface that allows users to create forms and navigate easily to the appropriate screens for data analysis and collection.

GoResearch™ is an advanced and thoroughly validated online platform designed for electronic data capture (EDC), developed by 2KMM specifically for research initiatives like clinical and observational studies as well as patient registries. It boasts a comprehensive suite of features that facilitate these projects across multiple domains, including the customization of data flow and management of Adverse Events procedures, which includes automatic email alerts to safety teams. Additionally, it allows for random assignment to treatment groups via its integrated randomization module, enables data collection through tailored electronic case report forms (eCRF) to align with the specific needs of each study, and supports the integration of ePRO, eSource, and mHealth data through specialized mobile or web applications, as well as a versatile application programming interface (API). This platform ultimately aims to enhance the efficiency and accuracy of data management in research contexts.

FormFoundry is a versatile web-based platform designed for organizations to create specialized data collection applications that meet their specific requirements. Its advanced web form builder enables the effortless launch of native mobile applications for field workers, while its adaptable data platform provides a comprehensive overview of essential business operations. Developed to address weaknesses in data management, FormFoundry enhances the data collection process significantly. Equip your business with powerful form creation tools, custom asset management, and sophisticated workflow configurations, all tailored to suit your precise needs. Inefficient data handling, incorrectly labeled files, and data corruption can lead to significant challenges for any organization. Additionally, the combination of sluggish manual data entry and review processes may result in some companies falling behind in the rapidly evolving digital landscape, highlighting the necessity for modern solutions. By adopting FormFoundry, organizations can eliminate these hurdles and ensure they remain competitive in today's fast-paced environment.

Harness the power of electronic data capture with FormsCenter by Medforce Technologies, a software solution that streamlines the way businesses connect and monitor data. With FormsCenter, obtaining necessary information becomes a straightforward task, ensuring the accuracy of all collected data. This platform enables the centralized storage of extensive datasets, significantly minimizing the chances of information being overlooked. Additionally, users can conveniently export their data in multiple formats according to their needs. Data is the backbone of your business, and FormsCenter simplifies the process of capturing and utilizing crucial information efficiently. Say goodbye to handwritten forms and the hassle of repetitive data entry. No longer will you need to manage your operations using uncoordinated, manual spreadsheets. You have the autonomy to determine what information your business requires, leveraging the extensive toolbox to create and modify forms tailored to your specific needs. With FormsCenter, you can collect and monitor data in a precise, consistent, and compliant manner, catering to both external sources and internal employees alike, ultimately enhancing overall productivity and data integrity. This innovative system not only supports better decision-making but also promotes a more organized approach to data management across your organization.

CORE (Clinical On-demand Research) provides a variety of specialized services that encompass the design, development, and management of electronic forms utilized in clinical trials both in the UK and internationally. In addition to crafting the necessary forms, CORE facilitates randomization, oversees data management, and supplies crucial study statistics, ensuring researchers have access to essential information. This organization is instrumental in collecting important data for those in both academic and commercial research environments. CORE has established a successful collaboration with FormsVision, which began under an FP7 EU funding initiative, and has implemented the ALEA eCRF (electronic Case Report Form) to enhance trials conducted in the UK and New Zealand. The dedicated team at CORE stands ready to provide an array of services, including database construction for CRFs, management of randomizations, drug supply coordination, and ePRO (ALEA). Furthermore, they offer data hosting solutions for various types of files, as well as expert guidance on funding applications, statistical support, and protocol writing advice. This comprehensive suite of services positions CORE as a vital partner in advancing clinical research efforts.

Gather various types of form information, including calculations with checks in place to guarantee thorough and precise outcomes. Capture electronic signatures either on your device or online, ensuring that these signatures are secure and digitally verified. You can take photos for documentation or upload images straight from your photo library, with the ability to annotate these images and incorporate them into sketches. Enhance your documents and photographs with additional drawings, graphics, and annotations for a more polished finish. naturalForms seamlessly integrates with a multitude of applications, streamlining your workflow and maximizing productivity. Effortlessly input data using features like a virtual keyboard, checkboxes, dropdown menus, radio buttons, and date and time selectors. You can also establish required fields or execute validation checks to confirm that the data you receive is both accurate and complete, enhancing the overall quality of your forms. This comprehensive approach not only simplifies the process but also fosters efficiency in data collection.

secuTrial® is a comprehensive, browser-based EDC system that adheres to GCP standards for gathering patient information in both clinical trials and non-interventional research, as well as patient registries. Since its inception in 2000, secuTrial® has been utilized in more than 600 studies and long-term projects globally, undertaken by universities, CROs, medical technology companies, and pharmaceutical organizations, highlighting its exceptional quality, versatility, and high levels of user satisfaction. This robust web-based software solution facilitates the collection and management of patient data for multi-center clinical studies entirely online. It guarantees compliance with all relevant licensing and data privacy laws while maintaining the highest quality benchmarks, ensuring that user needs are met effectively. The continued use of secuTrial® in diverse research settings underscores its reliability and the trust it has garnered in the scientific community.

Signant Health operates as a worldwide leader in evidence generation, striving to transform the landscape of clinical trials by connecting with patients in their environments and rethinking the route to validation. Their extensive range of clinical technology solutions includes electronic Clinical Outcome Assessments (eCOA), Electronic Data Capture (EDC), electronic clinician evaluations, and a cohesive eClinical platform. Additionally, they offer patient engagement solutions featuring a user-friendly app, eConsent for informed consent processes, and telemedicine functionalities. Furthermore, Signant Health delivers clinical data and analytics services, which include COA data analysis as well as the aggregation and interpretation of data. With a rich history spanning over three decades, they have played an instrumental role in supporting numerous trials and have been pivotal in hundreds of drug approvals, establishing themselves as a reliable ally for sponsors and CROs eager to provide high-quality data for informed trial decisions and regulatory submissions. Their commitment to innovation continues to shape the future of clinical research.

The integration of eCOA and digital technologies is paving the way for the future of clinical research, seamlessly connecting traditional methods with innovative, patient-centered approaches. Choose YPrime's eCOA solutions to not only obtain high-quality patient data but also to enhance the overall user experience for sponsors, investigator sites, and patients alike. By employing a flexible software development strategy, YPrime is able to swiftly tailor and adapt functionalities to meet specific study requirements within an impressive timeframe of 8 to 12 weeks. Our engaging and visual design process allows clients to review the system at various stages of development, ensuring they are informed before the system goes live. Additionally, our pre-validated and customizable authoring environment not only streamlines startup timelines but also accommodates post-production adjustments, such as changes to study protocols, making it an indispensable asset for clinical research. This commitment to agility and responsiveness positions YPrime as a leader in the evolving landscape of clinical trials.

Data management is crucial to the success and efficiency of your clinical research. Despite being complex, Quanta View, an e-CRF, makes it possible to control the processing of your data. Quanta View includes elements such as monitoring, follow up of inclusions, and project management. The application will be there to help you in all aspects of your clinical research. It is accessible via the internet and responsive. It adapts to all media (tablet, laptop, etc.). Quanta view is designed for the pharmaceutical, medical device, and cosmetic industries.

The Dell PowerEdge R series comprises enterprise-level rack servers that are specifically engineered for data centers and IT settings, delivering exceptional performance, scalability, and adaptability for a wide range of workloads. These servers come in various sizes, including 1U, 2U, and other configurations, and are equipped with powerful Intel or AMD processors, extensive memory options, and versatile storage solutions such as HDDs, SSDs, and NVMe drives. Furthermore, they facilitate expandability through multiple PCIe slots, include integrated management capabilities like iDRAC, and boast strong security measures along with energy-efficient components. Each model within the series offers distinctive features, making them suitable for applications ranging from virtualization and high-performance computing to robust database management and beyond. Overall, the Dell PowerEdge R series stands out as a reliable choice for organizations looking to enhance their IT infrastructure.

Establish the groundwork for an advanced Unified Fabric data center by utilizing the modular Cisco Nexus 7000 and 7700 switches, which provide a robust array of Cisco NX-OS functionalities along with open-source programming resources tailored for software-defined networking (SDN) implementations. These switches support high-density options for 10, 40, and 100 Gigabit Ethernet, equipped with features that enhance application awareness and performance analysis, ensuring optimal network efficiency and reliability. Furthermore, their modular design allows for scalability and flexibility in meeting evolving data center demands.

Transforming business documents into tangible business value is essential in today's digital landscape. By eliminating obstacles in document-heavy workflows, ABBYY FlexiCapture emerges as an Intelligent Document Processing platform tailored for the intricate demands of modern enterprises. This sophisticated platform unifies the finest capabilities in natural language processing, machine learning, and advanced document recognition, making it adept at handling various document types—ranging from straightforward forms to intricate free-form documents—and accommodating diverse workloads, from individual documents to extensive batches with strict service level agreements. FlexiCapture effectively orchestrates the entire process from document acquisition to final delivery, seamlessly integrating with content-driven business applications like RPA and BPM, which in turn allows organizations to concentrate on enhancing customer service, reducing costs, ensuring compliance, and gaining a competitive edge. As a result, an increasing number of companies are realizing substantial savings by leveraging Intelligent Process Automation to pinpoint automation opportunities, enabling them to operate more efficiently and effectively than ever before. This shift not only streamlines operations but also empowers businesses to innovate and adapt in a rapidly changing market.

Secure and user friendly cloud-based EDC platform for managing clinical trials and studies of all sizes and complexities: ePRO, eConsent, eCOA, eSource, PROMs, PREMs, functional health assessments and participant education/engagement.

Streamline your clinical studies with Clinvigilant, your global cost-effective eClinical tools provider for CROs, Pharma, Biotech, Nutraceuticals and Academic organizations in clinical and post-marketing stages. Most of our clients choose and stay with us for thanks to our: ♦ Fast EDC set-up (less than 4 weeks). ♦ Cost-effectiveness. ♦ 3rd party integrations (including legacy systems). Our cloud-based suite (Microsoft Azure) is HIPAA, ICH-GCP, GDPR & 21 CFR part 11 compliant and we have been audited by the FDA, EMA and MHRA. The Clinvigilant eClinical suite includes: EDC, CTMS, eCRF, eTMF, eSource, IWRS, ePRO, eConsent and eCOA. Just pick the tools that you need and we will integrate them within your existing software ecosystem. Every interaction and data exchange creates Audit Trails, which provide compliant real-time data visibility across all relevant roles. Our products are modular, highly customizable, and available on the web, iPad, and Mobile App for both Android and iOS. We also support Patient's Own Device (BYOD) and interface with Devices and Wearables. Clinvigilant💊, your one-stop🌐solutions provider for clinical trials☁️ .

Optimize the process of capturing, recognizing, and classifying business documents with IBM® Datacap software, an essential component of the IBM Cloud Pak® for Business Automation. This software enhances the efficiency of document management by utilizing advanced technologies, including natural language processing, text analytics, and machine learning, to identify, classify, and extract information from unstructured and variable paper documents. It accommodates input from multiple channels, such as scanners, faxes, emails, digital files like PDFs, and images sourced from applications and mobile devices. By leveraging machine learning, it automates the handling of complex or unfamiliar formats, making it easier to manage highly variable documents that traditional systems find challenging. Additionally, it allows for the export of documents and data to various applications and content repositories, both from IBM and other providers. Furthermore, users can quickly configure capture workflows and applications through an intuitive point-and-click interface, significantly accelerating the deployment process. This streamlined approach ultimately enhances productivity and ensures a more seamless document management experience.

Management of clinical data. Comprehensive solution for managing clinical trial information. Easy data entry and creation of CRFs. Support for multi-center complex studies. Data validation and processing is accelerated Multilingual capabilities. Global deployment, cloud-based and on-premise. Clinical researchers understand the importance of reducing time and costs when conducting clinical trials. This is especially true when it comes to the collection, processing, and management of study-specific data. To ensure that the necessary patient data was recorded and sent to the sponsor for analysis and processing, study coordinators used paper Case Report Forms (CRFs). The days of paper CRFs are long gone. The industry now understands that electronic data capture (EDC), systems increase efficiency and improve data quality.